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Refinado por: Base de dados/Biblioteca: EBSCO_MEDLINE Complete（医学期刊全文数据库） remover Base de dados/Biblioteca: Single Journals remover ROAD remover
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1
Mutations in the von Hippel-Lindau (VHL) tumor suppressor gene and VHL-haplotype analysis in patients with presumable congenital erythrocytosis
Mutations in the von Hippel-Lindau (VHL) tumor suppressor gene and VHL-haplotype analysis in patients with presumable congenital erythrocytosis
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Mutations in the von Hippel-Lindau (VHL) tumor suppressor gene and VHL-haplotype analysis in patients with presumable congenital erythrocytosis

Cario, H ; Schwarz, K ; Jorch, N ; Kyank, U ; Petrides, PE ; Schneider, DT ; Uhle, R ; Debatin, KM ; Kohne, E

Haematologica (Roma), 2005-01, Vol.90 (1), p.19-24 [Periódico revisado por pares]

Pavia: Haematologica

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2
Extent to which hairpin opening by the Artemis:DNA-PKcs complex can contribute to junctional diversity in V(D)J recombination
Extent to which hairpin opening by the Artemis:DNA-PKcs complex can contribute to junctional diversity in V(D)J recombination
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Extent to which hairpin opening by the Artemis:DNA-PKcs complex can contribute to junctional diversity in V(D)J recombination

Lu, Haihui ; Schwarz, Klaus ; Lieber, Michael R

Nucleic acids research, 2007-11, Vol.35 (20), p.6917-6923 [Periódico revisado por pares]

England: Oxford University Press

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3
Atypical familial hemophagocytic lymphohistiocytosis due to mutations in UNC13D and STXBP2 overlaps with primary immunodeficiency diseases
Atypical familial hemophagocytic lymphohistiocytosis due to mutations in UNC13D and STXBP2 overlaps with primary immunodeficiency diseases
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Atypical familial hemophagocytic lymphohistiocytosis due to mutations in UNC13D and STXBP2 overlaps with primary immunodeficiency diseases

ROHR, Jan ; BEUTEL, Karin ; WOESSMANN, Wilhelm ; GROLL, Andreas H ; STRAHM, Brigitte ; PAGEL, Julia ; SPECKMANN, Carsten ; JANKA, Gritta ; GRIFFITHS, Gillian ; SCHWARZ, Klaus ; ZUR STADT, Udo ; EHL, Stephan ; MAUL-PAVICIC, Andrea ; VRAETZ, Thomas ; THIEL, Jens ; WARNATZ, Klaus ; BONDZIO, Ilka ; GROSS-WIELTSCH, Ute ; SCHÜNDELN, Michael ; SCHÜTZ, Barbara

Haematologica (Roma), 2010-12, Vol.95 (12), p.2080-2087 [Periódico revisado por pares]

Pavia: Ferrata Storti Foundation

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4
The morphological diagnosis of congenital dyserythropoietic anemia: results of a quantitative analysis of peripheral blood and bone marrow cells
The morphological diagnosis of congenital dyserythropoietic anemia: results of a quantitative analysis of peripheral blood and bone marrow cells
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The morphological diagnosis of congenital dyserythropoietic anemia: results of a quantitative analysis of peripheral blood and bone marrow cells

HEIMPEL, Hermann ; KELLERMANN, Kerstin ; NEUSCHWANDER, Nadine ; HÖGEL, Josef ; SCHWARZ, Klaus

Haematologica (Roma), 2010-06, Vol.95 (6), p.1034-1036 [Periódico revisado por pares]

Pavia: Ferrata Storti Foundation

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5
Tissue-specific translational regulation of alternative rabbit 15-lipoxygenase mRNAs differing in their 3′-untranslated regions
Tissue-specific translational regulation of alternative rabbit 15-lipoxygenase mRNAs differing in their 3′-untranslated regions
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Tissue-specific translational regulation of alternative rabbit 15-lipoxygenase mRNAs differing in their 3′-untranslated regions

Thiele, Bernd-Joachim ; Berger, Mario ; Huth, Antje ; Reimann, Iris ; Schwarz, Kristin ; Thiele, Holger

Nucleic acids research, 1999-04, Vol.27 (8), p.1828-1836 [Periódico revisado por pares]

England: Oxford University Press

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6
Molecular genetic analyses in familial and sporadic congenital primary erythrocytosis
Molecular genetic analyses in familial and sporadic congenital primary erythrocytosis
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Molecular genetic analyses in familial and sporadic congenital primary erythrocytosis

Rives, Susana ; Pahl, Heike L ; Florensa, Lourdes ; Bellosillo, Beatriz ; Neusuess, Andrea ; Estella, Jesus ; Debatin, Klaus-Michael ; Kohne, Elisabeth ; Schwarz, Klaus ; Cario, Holger

Haematologica (Roma), 2007-05, Vol.92 (5), p.674-677 [Periódico revisado por pares]

Pavia: Haematologica

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7
A new type of transfusion-dependent congenital dyserythropoietic anemia
A new type of transfusion-dependent congenital dyserythropoietic anemia
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A new type of transfusion-dependent congenital dyserythropoietic anemia

Heimpel, Hermann ; Kohne, Elisabeth ; Schrod, Lothar ; Schwarz, Klaus ; Wickramasinghe, Sunitha

Haematologica (Roma), 2007-10, Vol.92 (10), p.1427-1428 [Periódico revisado por pares]

Pavia: Haematologica

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8
Tissue-specific translational regulation of alternative rabbit 15-lipoxygenase mRNAs differing in their 3 theta -untranslated regions
Tissue-specific translational regulation of alternative rabbit 15-lipoxygenase mRNAs differing in their 3 theta -untranslated regions
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Tissue-specific translational regulation of alternative rabbit 15-lipoxygenase mRNAs differing in their 3 theta -untranslated regions

Thiele, B-J ; Berger, M ; Huth, A ; Reimann, I ; Schwarz, K ; Thiele, H

Nucleic acids research, 1999-04, Vol.27 (8), p.1828-1836 [Periódico revisado por pares]

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9
Improved yields of long PCR products using gene 32 protein
Improved yields of long PCR products using gene 32 protein
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Improved yields of long PCR products using gene 32 protein

SCHWARZ, K ; HANSEN-HAGGE, T ; BARTRAM, C

Nucleic acids research, 1990-02, Vol.18 (4), p.1079-1079 [Periódico revisado por pares]

Oxford: Oxford University Press

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10
Ancient DNA from European early neolithic farmers reveals their near eastern affinities
Ancient DNA from European early neolithic farmers reveals their near eastern affinities
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Ancient DNA from European early neolithic farmers reveals their near eastern affinities

Haak, Wolfgang ; Balanovsky, Oleg ; Sanchez, Juan J ; Koshel, Sergey ; Zaporozhchenko, Valery ; Adler, Christina J ; Der Sarkissian, Clio S I ; Brandt, Guido ; Schwarz, Carolin ; Nicklisch, Nicole ; Dresely, Veit ; Fritsch, Barbara ; Balanovska, Elena ; Villems, Richard ; Meller, Harald ; Alt, Kurt W ; Cooper, Alan Penny, David

PLoS biology, 2010-11, Vol.8 (11), p.e1000536-e1000536 [Periódico revisado por pares]

United States: Public Library of Science

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